Validation Engineer - Contract

DISHER • Grand Rapids, MI

2d • Hybrid

About The Position

DISHER is seeking an experienced Validation Engineer to support a customer team with engineering work to develop and execute IQ/OQ/PQ process validation. The engineer will help develop a Validation Master Plan (VMP), prepare protocols and supporting documents, and execute process validation. This is a hybrid position with onsite work in Grand Rapids as needed. The expected duration is 8 weeks, with the potential to extend. The role is scheduled for 40 hours per week.

Requirements

• Bachelor's degree in Quality Engineering, Validation Engineering, or a related engineering discipline.
• Experience developing Validation Master Plans.
• Experience developing validation processes (IQ/OQ/PQ).
• Ability to document protocols, process validation, quality plans, work instructions, and related materials.
• Ability to work onsite in Grand Rapids as needed.

Nice To Haves

• 1–5 years of medical device experience preferred.

Responsibilities

• Develop a Validation Master Plan (VMP).
• Develop protocols and supporting documents and execute process validation (IQ, OQ, PQ).
• Prepare documentation, including protocols, IQ/OQ/PQ documents, quality plans, work instructions, label masters, quality inspection documents, and testing documentation.
• Work 40 hours per week and go onsite in Grand Rapids as needed.

What This Job Offers

• Career Level: Mid Level